A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17606804



Internal ID21798851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:102097383..102097507hg38UCSC Ensembl
chr12:102491161..102491285hg19UCSC Ensembl
Cytoband12q23.2
Allele length
AssemblyAllele length
hg38125
hg19125
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6025222
Supporting Variants
Samples
Known GenesNUP37
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17606804
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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